Cloning of human GAP 43: Growth association and ischemic resurgence
Abstract
GAP-43 is a growth cone protein expressed in neurons especially during periods of axonal elongation. Poor repair in the adult mammalian CNS has been ascribed to restraints upon its expression. We have cloned human GAP-43 cDNA to investigate its potential involvement in neurological illness. Analysis of postmortem human brain tissue disclosed uniformly high expression of GAP-43 throughout the neonatal brain, whereas in the adult brain high levels of GAP-43 persist only in discrete regions. However, in the wake of ischemic injury in the adult brain, regions normally low in GAP-43 reexpress it at high levels, suggesting a role for GAP-43 in remodeling and repair of mature CNS neurons.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
After stroke, axonal sprouting has been demonstrated in mice, rats and non-human primates.
“After stroke, axonal sprouting has been demonstrated in mice, rats and non-human primates1–4,10,38.”
From GDF10 is a signal for axonal sprouting and functional recovery after stroke (2015) · cites this paper as [38]
PTEN inhibition potentiates axonal sprouting in optic nerve injury and spinal cord injury, through induction of PI3kinase signaling and activation of mTOR.
“PTEN inhibition potentiates axonal sprouting in optic nerve injury and spinal cord injury, through induction of PI3kinase signaling and activation of mTOR.”
From GDF10 is a signal for axonal sprouting and functional recovery after stroke (2015) · cites this paper as [38]
Inhibition of SOCS3 further promotes axonal sprouting on top of PTEN inhibition.
“Inhibition of SOCS3 further promotes axonal sprouting on top of PTEN inhibition8,37,38.”
From GDF10 is a signal for axonal sprouting and functional recovery after stroke (2015) · cites this paper as [38]
Cites
DNA sequencing with chain-terminating inhibitors
Sanger, F., Nicklen, S., & Coulson, A. R. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5463 · Cited by 68,572 · see citing works
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
Feinberg, A. P., & Vogelstein, B. (1983) · Analytical Biochemistry · doi:10.1016/0003-2697(83)90418-9 · Cited by 24,512 · see citing works
Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
Chirgwin, J. M., Przybyla, A., MacDonald, R. J., & Rutter, W. J. (1979) · Biochemistry · doi:10.1021/bi00591a005 · Cited by 21,725 · see citing works
Melton, D. A., Krieg, P. A., Rebagliati, M. R., Maniatis, T., Zinn, K., & Green, M. R. (1984) · Nucleic Acids Research · doi:10.1093/nar/12.18.7035 · Cited by 6,324 · see citing works
Shaw, G. D., & Kamen, R. (1986) · Cell · doi:10.1016/0092-8674(86)90341-7 · Cited by 3,946 · see citing works
Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information
Zuker, M., & Stiegler, P. (1981) · Nucleic Acids Research · doi:10.1093/nar/9.1.133 · Cited by 3,604 · see citing works
Degeneration and Regeneration of the Nervous System.
(1929) · JAMA · doi:10.1001/jama.1929.02710220063037 · Cited by 2,920 · see citing works
Pain and Its Effects in the Human Neonate and Fetus
Anand, K. J. S., & Hickey, P. R. (1987) · New England Journal of Medicine · doi:10.1056/nejm198711193172105 · Cited by 1,715 · see citing works
Lantos, P. L. (1985) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.48.5.496 · Cited by 1,154 · see citing works
The long and the short of long–term memory—a molecular framework
Goelet, P., Castellucci, V. F., Schacher, S., & Kandel, E. R. (1986) · Nature · doi:10.1038/322419a0 · Cited by 1,034 · see citing works
Synaptic release of excitatory amino acid neurotransmitter mediates anoxic neuronal death
Rothman, S. M. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-07-01884.1984 · Cited by 884 · see citing works
Skene, J. H. P., & Willard, M. B. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.89.1.96 · Cited by 583 · see citing works
Chang, F., & Greenough, W. T. (1984) · Brain Research · doi:10.1016/0006-8993(84)91008-4 · Cited by 523 · see citing works
Meiri, K. F., Pfenninger, K. H., & Willard, M. B. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.10.3537 · Cited by 522 · see citing works
A Protein Induced During Nerve Growth (GAP-43) is a Major Component of Growth-Cone Membranes
Skene, J. H. P., Jacobson, R. D., Snipes, G. J., McGuire, C. B., Norden, J. J., & Freeman, J. A. (1986) · Science · doi:10.1126/science.3738509 · Cited by 513 · see citing works
Changes in axonally transported proteins during axon regeneration in toad retinal ganglion cells.
Skene, J. H. P., & Willard, M. B. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.89.1.86 · Cited by 492 · see citing works
Extensive elongation of axons from rat brain into peripheral nerve grafts
Benfey, M., & Aguayo, A. J. (1982) · Nature · doi:10.1038/296150a0 · Cited by 445 · see citing works
Jacobson, R., Virág, I., & Skene, J. H. P. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-06-01843.1986 · Cited by 434 · see citing works
Morphological Basis of Long-Term Habituation and Sensitization in Aplysia
Bailey, C. H., & Chen, M. (1983) · Science · doi:10.1126/science.6828885 · Cited by 420 · see citing works
Experimental and Clinical Neurotoxicology
Rosenberg, R. N. (1981) · Neurology · doi:10.1212/wnl.31.3.369-a · Cited by 410 · see citing works
Primary structure and transcriptional regulation of GAP-43, a protein associated with nerve growth
Basi, G. S., Jacobson, R. D., Virág, I., Schilling, J., & Skene, J. H. P. (1987) · Cell · doi:10.1016/0092-8674(87)90616-7 · Cited by 355 · see citing works
Cloning of Complementary DNA for GAP-43, a Neuronal Growth-Related Protein
Karns, L. R., Ng, S., Freeman, J. A., & Fishman, M. C. (1987) · Science · doi:10.1126/science.2437653 · Cited by 349 · see citing works
Self-citationRegulation of calmodulin binding to P-57. A neurospecific calmodulin binding protein.
Alexander, K. A., Cimler, B. M., Meier, K. E., & Storm, D. R. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45544-5 · Cited by 333 · see citing works
Purification of a novel calmodulin-binding protein from bovine cerebral cortex membranes
Andreasen, T. J., Luetje, C. W., Heideman, W., & Storm, D. R. (1983) · Biochemistry · doi:10.1021/bi00289a001 · Cited by 225 · see citing works
Aloyo, V. J., Zwiers, H., & Gispen, W. H. (1983) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1983.tb04790.x · Cited by 221 · see citing works
Piechaczyk, M., Yang, J., Blanchard, J., Jeanteur, P., & Marcu, K. B. (1985) · Cell · doi:10.1016/0092-8674(85)90116-3 · Cited by 220 · see citing works
Benowitz, L. I., & Er, L. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-11-02153.1983 · Cited by 217 · see citing works
Nelson, R. B., & Routtenberg, A. (1985) · Experimental Neurology · doi:10.1016/0014-4886(85)90277-8 · Cited by 201 · see citing works
Protein kinase C phosphorylates a 47 Mr protein (F1) directly related to synaptic plasticity
Akers, R. F., & Routtenberg, A. (1985) · Brain Research · doi:10.1016/0006-8993(85)90576-1 · Cited by 183 · see citing works
Neve, R. L., Perrone‐Bizzozero, N. I., Finklestein, S. P., Zwiers, H., Bird, E., Kurnit, D. M., & Benowitz, L. I. (1987) · Molecular Brain Research · doi:10.1016/0169-328x(87)90012-x · Cited by 161 · see citing works
P-57 is a neural specific calmodulin-binding protein.
Cimler, B. M., Andreasen, T. J., Andreasen, K., & Storm, D. R. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)85150-5 · Cited by 150 · see citing works
Characterization of murine cDNAs encoding P-57, a neural-specific calmodulin-binding protein.
Cimler, B. M., Giebelhaus, D. H., Wakim, B. T., Storm, D. R., & Moon, R. T. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45330-6 · Cited by 124 · see citing works
Growth-associated proteins and the curious dichotomies of nerve regeneration
Skene, J. H. P. (1984) · Cell · doi:10.1016/0092-8674(84)90404-5 · Cited by 106 · see citing works
Neve, R. L., Perrone‐Bizzozero, N. I., Finklestein, S. P., Zwiers, H., BIRD, E., Kurnit, D. M., & Benowitz, L. I. (1987) · Brain Research · doi:10.1016/s0006-8993(87)80012-4 · Cited by 93 · see citing works
Molecular cloning of a functional bovine interleukin 2 cDNA.
Reeves, R., Spies, A., Nissen, M. S., Buck, C. D., Weinberg, A., Barr, P. J., Magnuson, N. S., & Magnuson, J. A. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.10.3228 · Cited by 67 · see citing works
(1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.23.9274 · Cited by 52 · see citing works
Belardetti, F., Schacher, S., Kandel, E. R., & Siegelbaum, S. A. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.18.7094 · Cited by 37 · see citing works
Biology of the Nerve Growth Cone
Gordon‐Weeks, P. R. (1986) · Trends in Neurosciences · doi:10.1016/0166-2236(86)90100-1 · Cited by 26 · see citing works
Biology of the nerve growth cone
Kater, S. B., & Letourneau, P. C. (1985) · Medical Entomology and Zoology · Cited by 24 · see citing works
Flagged first, then by citations
2 of the 41 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Plasticity during stroke recovery: from synapse to behaviour
Murphy, T. H., & Corbett, D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2735 · Cited by 1,938 · see citing works
Brain–computer interfaces in neurological rehabilitation
Daly, J. J., & Wolpaw, J. R. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70223-0 · Cited by 1,149 · see citing works
Axonal Growth-Associated Proteins
Skene, J. H. P. (1989) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.12.030189.001015 · Cited by 1,145 · see citing works
Cellular and molecular mechanisms of neural repair after stroke: making waves
Carmichael, S. T. (2006) · Annals of Neurology · doi:10.1002/ana.20845 · Cited by 595 · see citing works
Stroemer, R. P., Kent, T. A., & Hulsebosch, C. E. (1995) · Stroke · doi:10.1161/01.str.26.11.2135 · Cited by 514 · see citing works
G0 is a major growth cone protein subject to regulation by GAP-43
Strittmatter, S. M., Valenzuela, D., Kennedy, T. E., Neer, E. J., & Fishman, M. C. (1990) · Nature · doi:10.1038/344836a0 · Cited by 420 · see citing works
Self-citationPlasticity of Cortical Projections after Stroke
Carmichael, S. T. (2003) · The Neuroscientist · doi:10.1177/1073858402239592 · Cited by 378 · see citing works
Stroemer, R. P., Kent, T. A., & Hulsebosch, C. E. (1998) · Stroke · doi:10.1161/01.str.29.11.2381 · Cited by 349 · see citing works
Mechanisms for recovery of motor function following cortical damage
Nudo, R. J. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.10.004 · Cited by 332 · see citing works
Doster, S. K., Lozano, A. M., Aguayo, A. J., & Willard, M. B. (1991) · Neuron · doi:10.1016/0896-6273(91)90066-9 · Cited by 315 · see citing works
Oestreicher, A. B., Graan, P. N. E. D., Gispen, W. H., Verhaagen, J., & Schrama, L. H. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00043-9 · Cited by 290 · see citing works
Schaechter, J. D., Fricker, Z. P., Perdue, K. L., Helmer, K. G., Vangel, M. G., Greve, D. N., & Makris, N. (2009) · Human Brain Mapping · doi:10.1002/hbm.20770 · Cited by 288 · see citing works
Patterns of aberrant sprouting in alzheimer's disease
Masliah, E., Mallory, M. E., Hansen, L. A., Alford, M. F., Albright, T., DeTeresa, R. M., Terry, R. D., Baudier, J., & Saitoh, T. (1991) · Neuron · doi:10.1016/0896-6273(91)90170-5 · Cited by 245 · see citing works
Regulation of free calmodulin levels by neuromodulin: neuron growth and regeneration
Liu, Y., & Storm, D. R. (1990) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(90)90195-e · Cited by 232 · see citing works
Expression of the potent vasoconstrictor endothelin in the human central nervous system.
Lee, M. E., de la Monte, S. M., Ng, S., Bloch, K. D., & Quertermous, T. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114677 · Cited by 228 · see citing works
Self-citationProtein kinase C and its substrates
Liu, J. (1996) · Molecular and Cellular Endocrinology · doi:10.1016/0303-7207(95)03706-3 · Cited by 227 · see citing works
Hoffman, P. N. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-03-00893.1989 · Cited by 226 · see citing works
The Neuronal Growth-Associated Protein GAP-43 Induces Filopodia in Non-Neuronal Cells
Zuber, M. X., Goodman, D. W., Karns, L. R., & Fishman, M. C. (1989) · Science · doi:10.1126/science.2658062 · Cited by 218 · see citing works
Self-citationRC3/neurogranin, a postsynaptic calpacitin for setting the response threshold to calcium influxes
Gerendasy, D. D., & Sutcliffe, J. G. (1997) · Molecular Neurobiology · doi:10.1007/bf02740632 · Cited by 206 · see citing works
The temporal profile of 72-kDa heat-shock protein expression following global ischemia
Simon, R. P., Cho, H., Gwinn, R. P., & Lowenstein, D. H. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-03-00881.1991 · Cited by 204 · see citing works
Mukaetova‐Ladinska, E. B., García‐Sierra, F., Hurt, J., Gertz, H.-J., Xuereb, J. H., Hills, R., Brayne, C., Huppert, F. A., Paykel, E. S., McGee, M. A., et al. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)64573-7 · Cited by 187 · see citing works
de la Monte, S. M., Federoff, H. J., Ng, S., Grabczyk, E., & Fishman, M. C. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90279-4 · Cited by 187 · see citing works
Self-citationGAP‐43 as a plasticity protein in neuronal form and repair
Strittmatter, S. M., Vartanian, T. K., & Fishman, M. C. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230506 · Cited by 185 · see citing works
Self-citationGDF10 is a signal for axonal sprouting and functional recovery after stroke
Li, S., Nie, E. H., Yin, Y., Benowitz, L. I., Tung, S., Vinters, H. V., Bahjat, F. R., Stenzel-Poore, M. P., Kawaguchi, R., Coppola, G., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4146 · Cited by 181 · see citing works
“In humans, the initial cloning studies of GAP43, the paradigmatic neuronal growth cone marker, showed that it is induced in peri-infarct cortex after stroke 39 and increases cortical thickness in regions of cortical map plasticity during recovery 7 .”
Dual regulation of GAP-43 gene expression by nerve growth factor and glucocorticoids.
Federoff, H. J., Grabczyk, E., & Fishman, M. C. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)77633-9 · Cited by 181 · see citing works
Self-citationIn Vivo Calcium Imaging Reveals Functional Rewiring of Single Somatosensory Neurons after Stroke
Winship, I. R., & Murphy, T. H. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0622-08.2008 · Cited by 175 · see citing works
Tetzlaff, W., Zwiers, H., Lederis, K. P., Cassar, L., & Bisby, M. A. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-04-01303.1989 · Cited by 170 · see citing works
Mapping the development of the rat brain by GAP-43 immunocytochemistry
Dani, J. W., Armstrong, D. M., & Benowitz, L. I. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90190-y · Cited by 166 · see citing works
B‐50 (GAP‐43): Biochemistry and Functional Neurochemistry of a Neuron‐Specific Phosphoprotein
Coggins, P. J., & Zwiers, H. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb11398.x · Cited by 163 · see citing works
Li, S., & Carmichael, S. T. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.03.011 · Cited by 162 · see citing works
Brain macrophages stimulate neurite growth and regeneration by secreting thrombospondin
Chamak, B., Morandi, V., & Mallat, M. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490380213 · Cited by 155 · see citing works
Localization of the growth-associated phosphoprotein GAP-43 (B-50, F1) in the human cerebral cortex
Benowitz, L. I., Perrone-Bizzozero, N., Finklestein, S. P., & Bird, E. D. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-03-00990.1989 · Cited by 153 · see citing works
Role of the growth-associated protein B-50/GAP-43 in neuronal plasticity
Gispen, W. H., Nielander, H. B., Graan, P. N. E. D., Oestreicher, A. B., Schrama, L. H., & Schotman, P. (1991) · Molecular Neurobiology · doi:10.1007/bf02935540 · Cited by 153 · see citing works
Transfection of PC12 cells with the human GAP-43 gene: effects on neurite outgrowth and regeneration
Yankner, B. A., Benowitz, L. I., Villa‐Komaroff, L., & Neve, R. L. (1990) · Molecular Brain Research · doi:10.1016/0169-328x(90)90071-k · Cited by 147 · see citing works
Emergent properties of neural repair: elemental biology to therapeutic concepts
Carmichael, S. T. (2016) · Annals of Neurology · doi:10.1002/ana.24653 · Cited by 144 · see citing works
Post-stroke remodeling processes in animal models and humans
Cirillo, C., Brihmat, N., Castel-Lacanal, E., Friec, A. L., Barbieux‐Guillot, M., Raposo, N., Pariente, J., Viguier, A., Simonetta‐Moreau, M., Albucher, J., et al. (2019) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19882788 · Cited by 133 · see citing works
Xin, H., Liu, Z., Buller, B., Li, Y., Golembieski, W., Gan, X., Wang, F., Lü, M., Ali, M. M., Zhang, Z. G., et al. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20950489 · Cited by 132 · see citing works
Local Hemodynamics Dictate Long-Term Dendritic Plasticity in Peri-Infarct Cortex
Mostany, R., Chowdhury, T. G., Johnston, D. G., Portonovo, S. A., Carmichael, S. T., & Portera‐Cailliau, C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3908-10.2010 · Cited by 122 · see citing works
Neurite outgrowth in PC12 cells deficient in GAP-43
Baetge, E. E., & Hammangt, J. P. (1991) · Neuron · doi:10.1016/0896-6273(91)90118-j · Cited by 116 · see citing works
Hooff, C. O. M. V., Holthuis, J. C. M., Oestreicher, A. B., Boonstra, J., Graan, P. N. E. D., & Gispen, W. H. (1989) · The Journal of Cell Biology · doi:10.1083/jcb.108.3.1115 · Cited by 115 · see citing works
B‐50/GAP43 Expression Correlates with Process Outgrowth in the Embryonic Mouse Nervous System
Biffo, S., Verhaagen, J., Schrama, L. H., Schotman, P., Danho, W., & Margolis, F. L. (1990) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1990.tb00440.x · Cited by 111 · see citing works
Remodeling of the Axon Initial Segment After Focal Cortical and White Matter Stroke
Hinman, J. D., Rasband, M. N., & Carmichael, S. T. (2012) · Stroke · doi:10.1161/strokeaha.112.668749 · Cited by 105 · see citing works
Benowitz, L. I., & Perrone‐Bizzozero, N. I. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)61716-1 · Cited by 106 · see citing works
Meberg, P. J., & Routtenberg, A. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90284-u · Cited by 103 · see citing works
Adult cortical plasticity following injury: Recapitulation of critical period mechanisms?
Nahmani, M., & Turrigiano, G. G. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.029 · Cited by 95 · see citing works
Selective conservation of GAP-43 structure in vertebrate evolution
LaBate, M., & Skene, J. H. P. (1989) · Neuron · doi:10.1016/0896-6273(89)90254-7 · Cited by 96 · see citing works
The 3 Rs of Stroke Biology: Radial, Relayed, and Regenerative
Carmichael, S. T. (2015) · Neurotherapeutics · doi:10.1007/s13311-015-0408-0 · Cited by 90 · see citing works
Irwin, N. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.6.1281 · Cited by 86 · see citing works
Emery, D. L., Royo, N. C., Fischer, I., Saatman, K. E., & McIntosh, T. K. (2003) · Journal of Neurotrauma · doi:10.1089/089771503322686085 · Cited by 81 · see citing works
de la Fuente, M. I., Colman, H., Rosenthal, M. A., Tine, B. A. V., Levacic, D., Walbert, T., Gan, H. K., Vieito, M., Milhem, M. M., Lipford, K., et al. (2022) · Neuro-Oncology · doi:10.1093/neuonc/noac139 · Cited by 82 · see citing works
Noh, M., Kwon, H. S., Kwon, M., Nahm, M., Jin, H. K., Bae, J., & Kim, S. H. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00867-4 · Cited by 85 · see citing works
Callahan, L. M., & Coleman, P. D. (1995) · Neurobiology of Aging · doi:10.1016/0197-4580(95)00035-d · Cited by 77 · see citing works
Regulated Binding of the Protein Kinase C Substrate GAP-43 to the V0/C2 Region of Protein Kinase C-δ
Dekker, L. V., & Parker, P. J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.19.12747 · Cited by 77 · see citing works
Acute increase in expression of growth associated protein GAP-43 following cortical ischemia in rat
Stroemer, R. P., Kent, T. A., & Hulsebosch, C. E. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90557-2 · Cited by 76 · see citing works
The Synaptic Pathology of Schizophrenia: Is Aberrant Neurodevelopment and Plasticity to Blame?
Eastwood, S. L. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59003-7 · Cited by 75 · see citing works
Lam, D. Y., Kaufman, P. L., Gabelt, B. T., To, E. C., & Matsubara, J. A. (2003) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.02-0779 · Cited by 74 · see citing works
Chapter 26 GAP-43 as a marker for structural plasticity in the mature CNS
Benowitz, L. I., Perrone‐Bizzozero, N. I., Neve, R. L., & Rodriguez, W. R. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)63187-8 · Cited by 72 · see citing works
Spencer, S. A., Schuh, S. M., Liu, W. S., & Willard, M. B. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50388-x · Cited by 71 · see citing works
Hippocampal and cortical growth-associated protein-43 messenger RNA in schizophrenia
Eastwood, S. L., & Harrison, P. J. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00040-2 · Cited by 70 · see citing works
Pan, R., Cai, J., Zhan, L., Guo, Y., Huang, R., Li, X., Zhou, M., Xu, D., Zhan, J., & Chen, H. (2017) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-017-1680-9 · Cited by 70 · see citing works
Aberrant GAP-43 gene expression in Alzheimer's disease.
de la Monte, S. M., Ng, S., & Hsu, D. (1995) · Europe PMC (PubMed Central) · Cited by 66 · see citing works
Self-citationGap-43 — What does it do in the growth cone?
Gordon‐Weeks, P. R. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90073-8 · Cited by 64 · see citing works
Sist, B., Fouad, K., & Winship, I. R. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.11.019 · Cited by 64 · see citing works
In situ hybridization histochemistry and the study of gene expression in the human brain
Harrison, P. J., & PEARSON, R. (1990) · Progress in Neurobiology · doi:10.1016/0301-0082(90)90007-4 · Cited by 61 · see citing works
Perrone‐Bizzozero, N. I., Neve, R. L., Irwin, N., Lewis, S., Fischer, I., & Benowitz, L. I. (1991) · Molecular and Cellular Neuroscience · doi:10.1016/1044-7431(91)90027-l · Cited by 62 · see citing works
Franzmeier, N., Dehsarvi, A., Steward, A., Biel, D., Dewenter, A., Roemer, S. N., Wagner, F., Groß, M., Brendel, M., Moscoso, A., et al. (2024) · Nature Communications · doi:10.1038/s41467-023-44374-w · Cited by 61 · see citing works
Identification of two promoter regions in the rat B-50/GAP-43 gene
Eggen, B. J. L., Nielander, H. B., Rensen, M. G. A., Schotman, P., Gispen, W. H., & Schrama, L. H. (1994) · Molecular Brain Research · doi:10.1016/0169-328x(94)90229-1 · Cited by 60 · see citing works
The Relationship of GAP‐43 to the Development and Plasticity of Synaptic Connectionsa
Benowitz, L. I., & Perrone‐Bizzozero, N. I. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb25914.x · Cited by 59 · see citing works
Yao, G. L., Kiyama, H., & Tohyama, M. (1993) · Molecular Brain Research · doi:10.1016/0169-328x(93)90168-o · Cited by 58 · see citing works
How is protein kinase C activated in CNS
Huang, K., & Huang, F. L. (1993) · Neurochemistry International · doi:10.1016/0197-0186(93)90037-6 · Cited by 57 · see citing works
An Imperfect Dopaminergic Error Signal Can Drive Temporal-Difference Learning
Potjans, W., Diesmann, M., & Morrison, A. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1001133 · Cited by 54 · see citing works
Baekelandt, V., Arckens, L., Annaert, W. G., Eysel, U. T., Orban, G. A., & Vandesande, F. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00987.x · Cited by 53 · see citing works
Robbins, M., & McKinney, M. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90047-f · Cited by 51 · see citing works
GAP-43 in the axons of mammalian CNS neurons regenerating into peripheral nerve grafts
Campbell, G., Anderson, P. N., Turmaine, M., & Lieberman, A. R. (1991) · Experimental Brain Research · doi:10.1007/bf00228507 · Cited by 50 · see citing works
Campagne, M. V. L., Oestreicher, A. B., Henegouwen, P. M. P. V. B. E., & Gispen, W. H. (1990) · Journal of Neurocytology · doi:10.1007/bf01186822 · Cited by 44 · see citing works
Zeng, B., Anderson, P. N., Campbell, G., & Lieberman, A. R. (1994) · Europe PMC (PubMed Central) · Cited by 41 · see citing works
McKinney, M., & Robbins, M. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90066-k · Cited by 42 · see citing works
Coleman, P. D., Kazee, A. M., Lapham, L. W., Eskin, T. A., & Rogers, K. E. (1992) · Neurobiology of Aging · doi:10.1016/0197-4580(92)90085-c · Cited by 41 · see citing works
Baizer, L., Alkan, S., Stocker, K. M., & Ciment, G. (1990) · Molecular Brain Research · doi:10.1016/0169-328x(90)90074-n · Cited by 40 · see citing works
Cloning and Characterization of the Rat Gene Encoding GAP‐43
Grabczyk, E., Zuber, M. X., Federoff, H. J., Ng, S., Pack, A. M., & Fishman, M. C. (1990) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1990.tb00393.x · Cited by 39 · see citing works
Self-citationOkada, M., Kawagoe, Y., Sato, Y., Nozumi, M., Ishikawa, Y., Tamada, A., Yamazaki, H., Sekino, Y., Kanemura, Y., Shinmyo, Y., et al. (2021) · Molecular Brain · doi:10.1186/s13041-021-00755-0 · Cited by 37 · see citing works
Pediatric Peripheral Neuroectodermal Tumors, Oncogenes, and Differentiation
Thiele, C. J. (1990) · Cancer Investigation · doi:10.3109/07357909009018932 · Cited by 36 · see citing works
Translating the frontiers of brain repair to treatments: Starting not to break the rules
Carmichael, S. T. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.09.005 · Cited by 35 · see citing works
Presynaptic phosphoprotein B-50/GAP-43 in neuronal and synaptic plasticity.
Biewenga, J. E., Schrama, L. H., & Gispen, W. H. (1996) · Acta Biochimica Polonica · doi:10.18388/abp.1996_4502 · Cited by 33 · see citing works
Development of GAP-43 mRNA in the macaque cerebral cortex
Oishi, T., Higo, N., Umino, Y., Matsuda, K., & Hayashi, M. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00067-4 · Cited by 32 · see citing works
Klementiev, B., Novikova, T., Korshunova, I., Berezin, V., & Bock, E. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06245.x · Cited by 31 · see citing works
Transient expression of GAP-43 within the hippocampus after global brain ischemia in rat
Schmidt‐Kastner, R., Bedard, A. M., & Hakim, A. M. (1997) · Cell and Tissue Research · doi:10.1007/s004410050808 · Cited by 30 · see citing works
Cerebral venous thrombosis in nephrotic syndrome.
Akatsu, H., Vaysburd, M., Fervenza, F. C., Peterson, J., & Jacobs, M. B. (1997) · PubMed · Cited by 29 · see citing works
Wiese, U. H., Ruth, J. L., & Emson, P. C. (1992) · Brain Research · doi:10.1016/0006-8993(92)91669-6 · Cited by 29 · see citing works
Verhaagen, J., Zhang, Y., Hamers, F. P. T., & Gispen, W. H. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490350206 · Cited by 28 · see citing works
Transient expression of GAP-43 in nonneuronal cells of the embryonic chicken limb
Stocker, K. M., Baizer, L., & Ciment, G. (1992) · Developmental Biology · doi:10.1016/0012-1606(92)90295-r · Cited by 27 · see citing works
Jacobs, K. M., Neve, R. L., & Donoghue, J. P. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903360112 · Cited by 26 · see citing works
Himmelseher, S., Pfenninger, E. G., Kochs, E. F., & Auchter, M. (2000) · Journal of Neurosurgical Anesthesiology · doi:10.1097/00008506-200004000-00003 · Cited by 25 · see citing works
Cloning and promoter analysis of the human B-50/GAP-43 gene
de Groen, P. C., Eggen, B. J. L., Gispen, W. H., Schotman, P., & Schrama, L. H. (1995) · Journal of Molecular Neuroscience · doi:10.1007/bf02736770 · Cited by 24 · see citing works
Florez, J. C., Nelson, R. B., & Routtenberg, A. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90126-w · Cited by 23 · see citing works
Prévot, V., Bouret, S. G., Croix, D., Alonso, G., Jennes, L., Mitchell, V. A., Routtenberg, A., & Beauvillain, J. (2000) · Endocrinology · doi:10.1210/en.141.5.1648 · Cited by 22 · see citing works
Increased F1/GAP-43 mRNA Accumulation in Gerbil Hippocampus after Brain Ischemia
Tagaya, M., Matsuyama, T., Nakamura, H., Hata, R., Shimizu, S., Kiyama, H., Matsumoto, M., & Sugita, M. (1995) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1995.140 · Cited by 22 · see citing works
Neve, R. L., Ivins, K. J., Benowitz, L. I., During, M. J., & Geller, A. I. (1991) · Molecular Neurobiology · doi:10.1007/bf02935542 · Cited by 22 · see citing works
Coleman, P. D., Rogers, K. E., & Flood, D. G. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)63168-4 · Cited by 21 · see citing works
Kumagai, C., Tohda, M., Isobe, M., & Nomura, Y. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb08873.x · Cited by 21 · see citing works
- Authors
- Ng, S.-C., de la Monte, S. M., Conboy, G. L., Karns, L. R., & Fishman, M. C.
- Affiliations
- Howard Hughes Medical Institute (US)
- ORCID
- Fishman, Mark C.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1988-04
- Volume
- 1
- Issue
- 2
- Pages
- 133-139
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2054092941
- Cited by
- 150
- References
- 41
- Citations by year
- 2025: 4 · 2024: 1 · 2022: 1 · 2021: 9 · 2020: 1 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 4 · 2012: 1
- FWCI
- 6.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- GAP-43, growth-associated protein, cDNA cloning, growth cones, axon elongation, CNS repair, ischemic injury, neuronal remodeling, postmortem brain, neonatal brain, neurological disorders
- MeSH terms
- Adolescent, Aging, Amino Acid Sequence, Base Sequence, Brain, Cerebral Infarction, DNA, Humans, Infant, Newborn, Membrane Glycoproteins, Middle Aged, Molecular Sequence Data, Nerve Tissue Proteins, GAP-43 Protein
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review